Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23415055G>A | CA016148 | MYH7 | c.5499C>T (p.Asn1833=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23415055G>C | CA389035121 | MYH7 | c.5499C>G (p.Asn1833Lys) | |
14 | g.23415055G= | CA2123461760 | MYH7 | c.5499C= (p.Asn1833=) | |
14 | g.23415055G>T | CA389035120 | MYH7 | c.5499C>A (p.Asn1833Lys) | ClinVar |
14 | g.23415056T>A | CA389035122 | MYH7 | c.5498A>T (p.Asn1833Ile) | |
14 | g.23415056T>C | CA046966 | MYH7 | c.5498A>G (p.Asn1833Ser) | dbSNP ExAC gnomAD v2 |
14 | g.23415056T>G | CA389035123 | MYH7 | c.5498A>C (p.Asn1833Thr) | |
14 | g.23415056T= | CA2123461766 | MYH7 | c.5498A= (p.Asn1833=) | |
14 | g.23415057T>A | CA389035124 | MYH7 | c.5497A>T (p.Asn1833Tyr) | |
14 | g.23415057T>C | CA389035125 | MYH7 | c.5497A>G (p.Asn1833Asp) | |
14 | g.23415057T>G | CA389035126 | MYH7 | c.5497A>C (p.Asn1833His) | |
14 | g.23415058G>A | CA485765912 | MYH7 | c.5496C>T (p.Arg1832=) | dbSNP gnomAD v4 |
14 | g.23415058G>C | CA485765913 | MYH7 | c.5496C>G (p.Arg1832=) | |
14 | g.23415058G= | CA2123461770 | MYH7 | c.5496C= (p.Arg1832=) | |
14 | g.23415058G>T | CA485765914 | MYH7 | c.5496C>A (p.Arg1832=) | |
14 | g.23415059C>A | CA389035127 | MYH7 | c.5495G>T (p.Arg1832Leu) | |
14 | g.23415059C= | CA2123461780 | MYH7 | c.5495G= (p.Arg1832=) | |
14 | g.23415059C>G | CA389035128 | MYH7 | c.5495G>C (p.Arg1832Pro) | |
14 | g.23415059C>T | CA016140 | MYH7 | c.5495G>A (p.Arg1832His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23415060G>A | CA016134 | MYH7 | c.5494C>T (p.Arg1832Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23415060G>C | CA046932 | MYH7 | c.5494C>G (p.Arg1832Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23415060G= | CA2123461785 | MYH7 | c.5494C= (p.Arg1832=) | |
14 | g.23415060G>T | CA389035129 | MYH7 | c.5494C>A (p.Arg1832Ser) | |
14 | g.23415061C>A | CA389035130 | MYH7 | c.5493G>T (p.Lys1831Asn) | ClinVar |
14 | g.23415061C>G | CA389035131 | MYH7 | c.5493G>C (p.Lys1831Asn) | |
14 | g.23415061C>T | CA485765915 | MYH7 | c.5493G>A (p.Lys1831=) | |
14 | g.23415062T>A | CA389035134 | MYH7 | c.5492A>T (p.Lys1831Met) | |
14 | g.23415062T>C | CA389035132 | MYH7 | c.5492A>G (p.Lys1831Arg) | |
14 | g.23415062T>G | CA389035133 | MYH7 | c.5492A>C (p.Lys1831Thr) | |
14 | g.23415063T>A | CA389035136 | MYH7 | c.5491A>T (p.Lys1831Ter) | |
14 | g.23415063T>C | CA389035138 | MYH7 | c.5491A>G (p.Lys1831Glu) | |
14 | g.23415063T>G | CA389035141 | MYH7 | c.5491A>C (p.Lys1831Gln) | |
14 | g.23415064C>A | CA389035143 | MYH7 | c.5490G>T (p.Gln1830His) | |
14 | g.23415064C>G | CA389035145 | MYH7 | c.5490G>C (p.Gln1830His) | |
14 | g.23415064C>T | CA485765920 | MYH7 | c.5490G>A (p.Gln1830=) | |
14 | g.23415065T>A | CA389035148 | MYH7 | c.5489A>T (p.Gln1830Leu) | |
14 | g.23415065T>C | CA257808876 | MYH7 | c.5489A>G (p.Gln1830Arg) | dbSNP |
14 | g.23415065T>G | CA389035151 | MYH7 | c.5489A>C (p.Gln1830Pro) | |
14 | g.23415065T= | CA2123461791 | MYH7 | c.5489A= (p.Gln1830=) | |
14 | g.23415066G>A | CA389035153 | MYH7 | c.5488C>T (p.Gln1830Ter) | gnomAD v4 |
14 | g.23415066G>C | CA389035155 | MYH7 | c.5488C>G (p.Gln1830Glu) | |
14 | g.23415066G>T | CA389035157 | MYH7 | c.5488C>A (p.Gln1830Lys) | |
14 | g.23415067C>A | CA389035161 | MYH7 | c.5487G>T (p.Glu1829Asp) | |
14 | g.23415067C>G | CA389035159 | MYH7 | c.5487G>C (p.Glu1829Asp) | |
14 | g.23415067C>T | CA485765922 | MYH7 | c.5487G>A (p.Glu1829=) | |
14 | g.23415068T>A | CA389035165 | MYH7 | c.5486A>T (p.Glu1829Val) | |
14 | g.23415068T>C | CA389035167 | MYH7 | c.5486A>G (p.Glu1829Gly) | |
14 | g.23415068T>G | CA389035169 | MYH7 | c.5486A>C (p.Glu1829Ala) | |
14 | g.23415069C>A | CA389035172 | MYH7 | c.5485G>T (p.Glu1829Ter) | |
14 | g.23415069C= | CA2123461794 | MYH7 | c.5485G= (p.Glu1829=) |